In a case with splenomegaly of unknown origin and features of hypersplenism, an interstitial 9q deletion was identified as a sole clonal abnormality of bone marrow cells. The meaning of 9q deletion as a primary change, as well as its clinical significance, are considered.
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| http://dx.doi.org/10.1016/0165-4608(92)90114-n | DOI Listing |
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